4.7 Article

Drug connectivity mapping and functional analysis reveal therapeutic small molecules that differentially modulate myelination

Journal

BIOMEDICINE & PHARMACOTHERAPY
Volume 145, Issue -, Pages -

Publisher

ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
DOI: 10.1016/j.biopha.2021.112436

Keywords

Oligodendrogenesis; Oligodendrocyte; Pharmacogenomics; The Library of Integrated; Network-Based Cellular Signatures; LINCS; Subventricular zone; Optic nerve; PI3K; Akt

Funding

  1. Biotechnology and Biological Sciences Research Council (BBSRC, UK) [BB/M029379/1]
  2. Medical Research Council (MRC, UK) [MR/P025811/1]
  3. Multiple Sclerosis Society of the UK [40]
  4. University of Portsmouth PhD Programme
  5. MSCA Seal of Excellence @ UNIPD
  6. NVIDIA Hardware Grant
  7. German Research Council [AZ/115/1-1, AZ/115/1-3]
  8. Swiss National Funds [P300PA_171224]

Ask authors/readers for more resources

This study highlights the importance of drug repurposing in promoting oligodendrocyte regeneration and myelin repair, and identifies compounds with concentration-dependent effects on oligodendrocytes using a combination of systems biology and neurobiological approaches. The research demonstrates the bipartite effect of LY294002 on oligodendrocytes, indicating the need for careful consideration of drug concentrations in therapeutic strategies for neurodegenerative disorders.
Disruption or loss of oligodendrocytes (OLs) and myelin has devastating effects on CNS function and integrity, which occur in diverse neurological disorders, including Multiple Sclerosis (MS), Alzheimer's disease and neuropsychiatric disorders. Hence, there is a need to develop new therapies that promote oligodendrocyte regeneration and myelin repair. A promising approach is drug repurposing, but most agents have potentially contrasting biological actions depending on the cellular context and their dose-dependent effects on intracellular pathways. Here, we have used a combined systems biology and neurobiological approach to identify compounds that exert positive and negative effects on oligodendroglia, depending on concentration. Notably, next generation pharmacogenomic analysis identified the PI3K/Akt modulator LY294002 as the most highly ranked small molecule with both pro- and anti-oligodendroglial concentration-dependent effects. We validated these in silico findings using multidisciplinary approaches to reveal a profoundly bipartite effect of LY294002 on the generation of OPCs and their differentiation into myelinating oligodendrocytes in both postnatal and adult contexts. Finally, we employed transcriptional profiling and signalling pathway activity assays to determine cell-specific mechanisms of action of LY294002 on oligodendrocytes and resolve optimal in vivo conditions required to promote myelin repair. These results demonstrate the power of multidisciplinary strategies in determining the therapeutic potential of small molecules in neurodegenerative disorders.

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